1-Oxacyclododeca-5,7,9,11-tetraene-2,3-dione

Details

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Internal ID 05f92b6c-3cb2-4b2b-80fb-21d30aebf0d1
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name 1-oxacyclododeca-5,7,9,11-tetraene-2,3-dione
SMILES (Canonical) C1C=CC=CC=CC=COC(=O)C1=O
SMILES (Isomeric) C1C=CC=CC=CC=COC(=O)C1=O
InChI InChI=1S/C11H10O3/c12-10-8-6-4-2-1-3-5-7-9-14-11(10)13/h1-7,9H,8H2
InChI Key FBDXELGWKPRIGI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O3
Molecular Weight 190.19 g/mol
Exact Mass 190.062994177 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 2.50
Atomic LogP (AlogP) 1.68
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Oxacyclododeca-5,7,9,11-tetraene-2,3-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.7566 75.66%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.7001 70.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9523 95.23%
OATP1B3 inhibitior + 0.9748 97.48%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7890 78.90%
P-glycoprotein inhibitior - 0.9884 98.84%
P-glycoprotein substrate - 0.9803 98.03%
CYP3A4 substrate - 0.6613 66.13%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8460 84.60%
CYP3A4 inhibition - 0.9782 97.82%
CYP2C9 inhibition - 0.9489 94.89%
CYP2C19 inhibition - 0.9198 91.98%
CYP2D6 inhibition - 0.9586 95.86%
CYP1A2 inhibition - 0.9195 91.95%
CYP2C8 inhibition - 0.9874 98.74%
CYP inhibitory promiscuity - 0.9657 96.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8287 82.87%
Carcinogenicity (trinary) Non-required 0.5575 55.75%
Eye corrosion + 0.7998 79.98%
Eye irritation + 0.9797 97.97%
Skin irritation + 0.7242 72.42%
Skin corrosion + 0.5683 56.83%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8120 81.20%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation + 0.5946 59.46%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.8089 80.89%
Acute Oral Toxicity (c) II 0.4007 40.07%
Estrogen receptor binding - 0.6487 64.87%
Androgen receptor binding - 0.5824 58.24%
Thyroid receptor binding - 0.8524 85.24%
Glucocorticoid receptor binding - 0.8390 83.90%
Aromatase binding + 0.6669 66.69%
PPAR gamma - 0.7171 71.71%
Honey bee toxicity - 0.8854 88.54%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.4641 46.41%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.55% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.71% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.30% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 80.59% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163194276
LOTUS LTS0028039
wikiData Q105104768